Results 21 to 30 of about 56,164 (276)

Hydrogen-Bonding Interactions in Luminescent Quinoline-Triazoles with Dominant 1D Crystals

open access: yesMolecules, 2017
Quinoline-triazoles 2-((4-(diethoxymethyl)-1H-1,2,3-triazol-1-yl)methyl)quinoline (1), 2-((4-(m-tolyl)-1H-1,2,3-triazol-1-yl)methyl)quinoline (2) and 2-((4-(p-tolyl)-1H-1,2,3-triazol-1-yl)methyl)quinoline (3) have been prepared with CuAAC click reactions
Shi-Qiang Bai   +2 more
doaj   +1 more source

SYNTHESIS OF CERTAIN NOVEL PYRIDOTHIOPYRANOQUINOLINES AS POTENTIAL ANTICANCER AGENTS

open access: yesZagazig Journal of Pharmaceutical Sciences, 2006
A series of ethyl 2-substituted aminopyrido [3',2': 5,6] thiopyrano [ 4,3,2-de] quinoline-1-carboxylate (VII)i-viii was obtained by reacting ethyl2-chloropyrido[3',2':5,6] thiopyrano [4,3,2-de] quinoline-1-carboxylate (VIa) with certain aromatic amines ...
Khaled El-Shemy   +4 more
doaj   +1 more source

Ultrasonic treated sludge for accelerating quinoline biodegradation

open access: yes上海师范大学学报. 自然科学版, 2018
In this work,ultrasound was used for treating sludge,and released organics was used as electron donors for accelerating quinoline biodegradation.Flask experimental results showed that quinoline removal rates are proportional to the biomass of treated and
Wang Youke   +4 more
doaj   +1 more source

Infrared-spectra and normal-coordinate analysis of quinoline and quinoline complexes

open access: yes, 2021
Normal coordinate analysis was performed on the vibrational spectra data of quinoline and the force field parameters of the free molecule were determined by the refinement of the corresponding parameters of benzene and pyridine molecules.
Akyuz, S   +4 more
core   +2 more sources

A review on quinoline hydrazone derivatives as a new class of potent antitubercular and anticancer agents

open access: yesBeni-Suef University Journal of Basic and Applied Sciences, 2017
Tuberculosis (TB) and Cancer remains a global public health problem in recent years. There is an urgent need for the screening of new bioactive molecules with new targets and with a different mechanism of action.
Mustapha C. Mandewale   +4 more
doaj   +1 more source

Synthesis and in-vitro studies of some new quinoline 1,3,4-thiadiazolo pyrimidin derivatives

open access: yesBulletin of the Chemical Society of Ethiopia, 2017
A series of eight new quinoline associated 1,3,4-thiadiazolo pyrimidin derivatives (5a-h) have been developed using 4-amino-8-fluoro-quinoline-3-carboxylic acid ethyl ester (1) as raw material and by involving 8-fluoro-4-methylsulfanylthiocarbonylamino ...
K. K. Valluri,   +4 more
doaj   +1 more source

Quinoline-Based Molecules Targeting c-Met, EGF, and VEGF Receptors and the Proteins Involved in Related Carcinogenic Pathways

open access: yesMolecules, 2020
The quinoline ring system has long been known as a versatile nucleus in the design and synthesis of biologically active compounds. Currently, more than one hundred quinoline compounds have been approved in therapy as antimicrobial, local anaesthetic ...
Annamaria Martorana   +2 more
doaj   +1 more source

Synthesis and Antimicrobial Evaluation of New Quinoline Derivatives [PDF]

open access: yes, 2021
Introduction: Heterocyclic compound quinoline, a very important category of heterocyclic compounds, and its derivatives have medicine properties. Quinoline contains element heterocyclic aromatic ring.
Jonny Kumar, Arvind Kumar
core   +1 more source

1‐Azabicyclo[1.1.0]butanes (ABBs) on the Map: Mechanistic Pathways for Catalytic Ring Opening and Functionalizations

open access: yesAngewandte Chemie, EarlyView.
Catalytic strain‐release ring opening and functionalizations of 1‐azabicyclo[1.1.0]butanes (ABBs) represent a promising strategy for accessing diverse azetidine products. These transformations proceed via polar pathways, radical pathways, and hybrid mechanisms that combine both.
James Shao‐Jiun Yang   +1 more
wiley   +2 more sources

Redox‐Neutral Vicinal Dialkylation of Aryl Boronic Esters via the Palladium/Norbornene Cooperative Catalysis

open access: yesAngewandte Chemie, EarlyView.
A new mode of the palladium/norbornene (Pd/NBE) cooperative catalysis, that is, redox‐neutral difunctionalization of aryl boronic esters with two electrophiles, has been developed, which can be used to streamline the preparation of a functionalized benzoazepane.
Rong Ye   +4 more
wiley   +2 more sources

Home - About - Disclaimer - Privacy